Quality Expert Medical Devices (m/f) Job ID: 10393


Our customer is a global pharmaceutical player with HQ in Basel

Ihre Aufgaben
  • Ensure technical development and manufacturing operations of assigned Medical Devices/Combination Products are conducted in accordance with Quality System requirements
  • Manage portfolio of assigned projects, support a discipline and/or provide a service on his/her own or with a team of associates
  • Ensure high product quality, regulatory compliance and operational efficiency
  • Write, review and approve deliverables (e.g. procedures, records, third party work, contractors, clinical trial material, components) and related tools (e.g. IT, document systems, training tools, facility validation) to ensure GMP compliance
  • Perform or support inspections and audits as required
  • Lead project related activities (e.g. development of new tools, processes)
  • Release of medical devices for clinical studies and commercial use
Ihr Anforderungsprofil
  • Graduate in Chemistry, Pharmacy, Microbiology or Biotechnology or another related science 
  • Extended knowlede of QMS is a must
  • At least 3 years of relevant work experience
  • Excellent knowledge of cGMP, working knowledge of medical device and combination product regulations, standards and guidelines
  • Good knowledge of medical device development and life-cycle management
Ihre Vorteile
  • Attractive location, Pharma-hub Basel
  • Long-term project with high possibilty of extension and/or follow-up projects
  • Act as Project Consultant in an international pharmaceutical company 
Auf Anfrage
Auf Anfrage
Timo Gunia
Sales Consultant
Fon +41 41 510 04 90
Timo Gunia
Sales Consultant
Fon +41 41 510 04 90
Mobile +41 79 320 34 36
Mail timo.gunia@theentourage.ch
Betreff Bewerbung für Job ID 10393 auf theentourage.de